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Completed Phase 3 Interventional Results available

Oral HYCAMTIN Plus Whole Brain Radiation Therapy In Treatment Of Brain Metastases Resulting From Non-Small Lung Cancer

ClinicalTrials.gov ID: NCT00390806

Public ClinicalTrials.gov record NCT00390806. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 7, 2026, 10:15 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Phase III, Open-Label Study of Oral Topotecan Plus Whole-Brain Radiation Therapy (WBRT) Compared With WBRT Alone in Patients With Brain Metastases From Non-Small Cell Lung Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The current prognosis for patients with metastatic brain cancer from NSCLC is very poor. The current standard treatment for this disease is radiation therapy to the brain. The goal of the current study is to test whether the combination of orally administered HYCAMTIN capsules and whole brain radiation therapy will prolong the survival time of patients with this potentially serious condition.

Study identification

NCT ID
NCT00390806
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
472 participants

Conditions and interventions

Interventions

Drug · Radiation

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2006 (Type not available)
Primary completion
Jul 2012 (Actual)
Completion
Sep 2013 (Actual)
Last update posted
Jan 20, 2014

2006 – 2013

United States locations

U.S. sites
46
U.S. states
24
U.S. cities
43
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35294 —
GSK Investigational Site Glendale Arizona 85304 —
GSK Investigational Site Hot Springs Arkansas 71913 —
GSK Investigational Site Anaheim California 92801 —
GSK Investigational Site Duarte California 91010-3000 —
GSK Investigational Site Pleasant Hill California 94523 —
GSK Investigational Site Aurora Colorado 80012 —
GSK Investigational Site Lakeland Florida 33805 —
GSK Investigational Site Tampa Florida 33606 —
GSK Investigational Site Tampa Florida 33612 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Elk Grove Village Illinois 60007 —
GSK Investigational Site Galesburg Illinois 61401 —
GSK Investigational Site Park Ridge Illinois 60068 —
GSK Investigational Site Rockford Illinois 61108 —
GSK Investigational Site Skokie Illinois 60077 —
GSK Investigational Site Indianapolis Indiana 46227 —
GSK Investigational Site Westwood Kansas 66205 —
GSK Investigational Site Paducah Kentucky 42003 —
GSK Investigational Site Metairie Louisiana 70006 —
GSK Investigational Site Minneapolis Minnesota 55455 —
GSK Investigational Site Jackson Mississippi 39216 —
GSK Investigational Site Columbia Missouri 65201 —
GSK Investigational Site Kansas City Missouri 64154 —
GSK Investigational Site Lincoln Nebraska 68510 —
GSK Investigational Site Las Vegas Nevada 89106 —
GSK Investigational Site Las Vegas Nevada 89135 —
GSK Investigational Site Albuquerque New Mexico 87109 —
GSK Investigational Site Albany New York 12206 —
GSK Investigational Site Buffalo New York 14215-1199 —
GSK Investigational Site Buffalo New York 14215 —
GSK Investigational Site The Bronx New York 10467 —
GSK Investigational Site Columbus Ohio 43235 —
GSK Investigational Site Eugene Oregon 97401-8122 —
GSK Investigational Site Charleston South Carolina 29403 —
GSK Investigational Site Bedford Texas 76022 —
GSK Investigational Site Corpus Christi Texas 78412 —
GSK Investigational Site Dallas Texas 75320-2510 —
GSK Investigational Site Duncanville Texas 75137 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Lubbock Texas 79415 —
GSK Investigational Site Sherman Texas 75090 —
GSK Investigational Site Sugarland Texas 77479 —
GSK Investigational Site Everett Washington 98201 —
GSK Investigational Site Vancouver Washington 98684 —
GSK Investigational Site Madison Wisconsin 53792 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 42 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00390806, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 20, 2014 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00390806 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →